Meningococcal B Vaccination - Information for healthcare professionals · 2019. 1. 14. ·...
Transcript of Meningococcal B Vaccination - Information for healthcare professionals · 2019. 1. 14. ·...
1
Meningococcal B vaccination Information for healthcare practitioners
Meningococcal B vaccination. Information for healthcare professionals
2
Contents Meningococcal B vaccination ....................................................................................................... 1
Information for healthcare practitioners .................................................................................... 1
Contents ....................................................................................................................................... 2
Change history ............................................................................................................................. 4
Introduction .................................................................................................................................. 5
Meningococcal disease ................................................................................................................ 5
Risk of meningococcal disease ................................................................................................ 5
The MenB vaccine (Bexsero) ....................................................................................................... 6
Vaccine excipients .................................................................................................................... 6
Vaccine response and efficacy .................................................................................................... 6
Duration of protection ............................................................................................................... 7
Cross protection against other meningococcal capsular groups .............................................. 8
Vaccine supply ......................................................................................................................... 8
Shelf life of Bexsero .................................................................................................................. 8
The Meningococcal B immunisation programme ......................................................................... 8
Schedule .................................................................................................................................. 8
Catch-up programme ................................................................................................................ 9
Infants born before 1 May 2015 ................................................................................................ 9
Infants aged 6 to 8 weeks of age ............................................................................................ 10
Children 2 years of age and older........................................................................................... 10
Adverse reactions commonly associated with the administration of Bexsero ............................ 11
Latex allergy ........................................................................................................................... 11
Prophylactic paracetamol ........................................................................................................... 11
Fever and the use of prophylactic paracetamol after vaccination ........................................... 11
Risk of fever when Bexsero is administered at the same time as other routine childhood
vaccines ................................................................................................................................. 12
Using prophylactic infant paracetamol suspension with Bexsero vaccine .............................. 13
Recommendations for premature babies ................................................................................ 14
Alerting parents to the need to buy paracetamol prior to vaccination ..................................... 15
Paracetamol product licencing ............................................................................................... 15
Meningococcal B vaccination. Information for healthcare professionals
3
Liquid paracetamol supply ...................................................................................................... 16
Ibuprofen as an alternative to paracetamol to reduce post-vaccination fever after Bexsero... 16
Incomplete dose of liquid paracetamol ................................................................................... 16
Administering oral rotavirus vaccine at the same time as liquid paracetamol ......................... 17
Vaccine preparation and administration ..................................................................................... 17
Preparing Bexsero vaccine ..................................................................................................... 17
Administering Bexsero vaccine with other vaccines ............................................................... 17
Administering Bexsero to infants less than 12 months of age ................................................ 18
Administering Bexsero at 12 months of age ........................................................................... 18
Administering multiple vaccines in one session ...................................................................... 19
Delaying vaccination ............................................................................................................... 19
Administering Bexsero at the same time as MenC or MenACWY vaccines ........................... 19
Vaccine administration errors ..................................................................................................... 20
Bexsero administered earlier than 8 weeks of age ................................................................. 20
Inadvertent early administration of second dose .................................................................... 20
Missed doses of Bexsero vaccine .......................................................................................... 21
Vaccine inadvertently administered to child born before 1 May 2015 ..................................... 22
Incomplete dose administered ................................................................................................ 22
Useful links ................................................................................................................................. 23
References ................................................................................................................................. 24
Meningococcal B vaccination. Information for healthcare professionals
4
Change history Version number Change details Date
01.00 • New information
document
2018
02.00 • Updated missed
doses of Bexsero
section
• Inserted hyperlinks
• Reference list
compiled
July 2021
Meningococcal B vaccination. Information for healthcare professionals
5
Introduction
In September 2015, a vaccine against meningococcal B disease (MenB) was added to the
childhood immunisation programme as part of the routine schedule in England. This document
provides further information for healthcare practitioners about the MenB vaccine Bexsero and
the MenB vaccine programme.
Meningococcal disease
Meningococcal disease is caused by invasive infection with the bacterium Neisseria
meningitidis. There are 12 identified capsular groups of which groups B, C, W and Y were
historically the most common in the UK. Since the introduction of the routine MenC vaccination
programme in 1999, cases of invasive meningococcal disease (IMD) in the UK due to capsular
group C have reduced significantly.
Prior to the introduction of the infant MenB and teenage MenACWY immunisation programme,
MenB was responsible for 58% (418 of 724) of all cases of IMD in 2014 to 2015 (1) with the
highest incidence being reported among infants, followed by toddlers and then adolescents
aged 15 to 19 (Guidance for public health management of meningococcal disease in the UK,
2019).
IMD most commonly presents as either meningitis or septicaemia, or a combination of both.
Meningococci commonly colonise the nasopharynx of humans and usually do not cause
invasive disease. Between 5% and 11% of adults and up to 25% of adolescents carry the
bacteria without any signs or symptoms of the disease. In infants and young children, the
carriage rate is low.
The meningococci are transmitted by respiratory aerosols, droplets or by direct contact with the
respiratory secretions of someone carrying the bacteria. The incubation period is from 2 to 7
days and the presentation of disease ranges from severe acute and overwhelming features, to
insidious with mild prodromal symptoms.
Risk of meningococcal disease
Meningococcal disease can affect all age groups, but the rates of disease are highest in
children under 2 years of age. Meningococcal cases increase from birth and peak at 5 months
before declining gradually until 24 months. Cases remain low until 12 years of age and then
gradually increase to a smaller peak at 18 years before declining again.
Meningococcal B vaccination. Information for healthcare professionals
6
Individuals with asplenia, splenic dysfunction or complement disorders are also at an increased
risk of IMD and should be immunised in accordance with the schedule for immunisation of
individuals with underlying medical conditions (Green Book chapter 7).
The latest epidemiological data is available on the Meningococcal disease: guidance, data and
analysis gov.uk webpage.
The MenB vaccine (Bexsero) Bexsero is the recommended vaccine for the routine infant immunisation programme and is
currently the only market authorised meningococcal B vaccine for infants in the UK.
Bexsero is a multi-component inactivated vaccine made from 3 Neisseria meningitidis
proteins produced by recombinant DNA technology (Neisseria meningitidis group B
NHBA fusion protein, Neisseria meningitidis group B NadA protein, Neisseria
meningitidis group B fHbp fusion protein) and a preparation of Neisseria meningitidis
capsular group B outer membrane vesicle (OMV) Neisseria meningitidis group B strain
NZ98/254).
Vaccine excipients
Bexsero does not contain thiomersal or porcine gelatine but the tip cap of the syringe may
contain natural rubber latex (see section on latex allergy). For a full list of excipients, healthcare
professionals should read the Manufacturer's summary of product characteristics (SPC).
Vaccine response and efficacy
Bexsero has been shown to be immunogenic in infants and toddlers. Clinical trials for Bexsero
in infants initially included 3 doses followed by a booster in the second year of life. However,
clinical trials indicate that 2 Bexsero doses given 2 months apart can induce protective
bactericidal antibodies (antibodies that kill the bacteria), against MenB in nearly all infants (2).
Vaccine responses will also be boosted after the 12 month dose. In the limited catch-up cohort
of infants born in May and June 2015, vaccine responses in 12 week olds receiving 2 priming
doses a month apart and 16 week olds receiving a single priming dose may have been lower
but will have been boosted by the 12 month dose.
Vaccine-induced antibodies have been shown to be bactericidal against most MenB strains
causing invasive disease in the UK. However, Bexsero was licensed on immunogenicity studies
Meningococcal B vaccination. Information for healthcare professionals
7
because the incidence of MenB disease was too low for clinical trials to provide a measure of
efficacy.
A number of countries such as Cuba, Norway and New Zealand have previously used MenB
vaccines derived from outer membrane vesicles (OMVs) of specific meningococcal B strains
responsible for large outbreaks in their respective countries. A key limitation of these vaccines is
that they mainly protect against specific MenB strains and do not provide broad cross-protection
against other MenB strains causing invasive disease. In New Zealand, vaccine effectiveness for
the OMV component of their vaccine was estimated to be 73%.
The cost-effectiveness model reviewed by the Joint Committee on Vaccination and
Immunisation (JCVI) assumed that 88% of meningococcal B strains causing invasive disease in
England would be covered by Bexsero and vaccine effectiveness against these strains would
be 95%.
Within 10 months of implementing Bexsero in to the UK infant immunisation programme, the
vaccine was found to be 83% effective against all MenB disease in vaccine eligible infants,
which was equivalent to 94% protection against the predicted 88% vaccine-preventable strains.
Moreover, Parikh and others (3) reported that MenB cases in the vaccine-eligible cohort had
nearly halved compared to the 4 years prior to Bexsero introduction.
Duration of protection
When reviewing all of the available evidence, the JCVI agreed the most plausible duration of
protection was thought to be 18 months following a 2 dose primary course and 36 months
following the additional booster dose administered at 12 months of age. These estimates were
based on the waning antibody responses observed in infant clinical trials.
Ladhani and others (4) further evaluated the effectiveness of 4CMenB in preventing invasive
meningococcal group B disease in 2020. This evaluation reported that the incidence of
meningococcal B disease in England was significantly lower in vaccine eligible cohorts than the
expected incidence. During the period under evaluation (September 2015 to August 2018), 169
cases of meningococcal group B disease were reported in the vaccine eligible cohorts and 277
cases were prevented. The authors concluded that protection after receipt of 2 doses plus a
booster dose was sustained for at least 2 years.
Bexsero should, therefore, protect infants and toddlers during their period of highest risk of
meningococcal B infection.
Meningococcal B vaccination. Information for healthcare professionals
8
Cross protection against other meningococcal capsular groups
Whilst Bexsero has broad coverage against most MenB strains causing IMD in England, it does
not offer complete protection and studies to demonstrate protection against other capsular
strains remain on-going. Although there is some evidence confirming protection against other
meningococcal capsular groups, including the current MenW strain responsible for the national
outbreak in the UK, individuals requiring protection against meningococcal serogroups A, C, W
and Y should receive the MenACWY conjugate vaccine and should not assume to be protected
against these capsular groups even if they have received a complete course of Bexsero.
Vaccine supply
Bexsero for use in the national programme should be ordered via the ImmForm website and
healthcare professionals should refer to this website and Vaccine update (the monthly
vaccination newsletter for health practitioners) for up to date information on vaccine availability.
Shelf life of Bexsero
Bexsero has a shelf life of 2 years when stored in its original packaging in a refrigerator within
the recommended temperature range of +2°C and +8°C. Bexsero should not be frozen. It is
recommended that health professionals only order what they need for a 2 to 4 week period.
To ensure vaccines are ordered, stored and monitored as per national recommendations,
healthcare professionals should familiarise themselves with the recommendations made in
Chapter 3 of the Green Book 'Storage, distribution and disposal of vaccines'.
The Meningococcal B immunisation programme Schedule
It is recommended that the first 2 doses of MenB vaccine be administered together with the
other primary immunisations at 8 weeks and 16 weeks and the third dose given on or after the
first birthday (2 + 1 schedule).
These recommendations differ from the Bexsero Summary of Product Characteristics and
healthcare professionals are reminded that where recommendations regarding vaccines given
Meningococcal B vaccination. Information for healthcare professionals
9
in the Green Book differ from those in the Summary of Product Characteristics for a particular
vaccine, the recommendations in the Green Book, which are based on current expert advice
received from the JCVI, should be followed.
The basis of the JCVI recommendation for a 2+1 schedule is from studies of clinical trials which
have shown that nearly all infants develop bactericidal antibodies against MenB vaccine
antigens following 2 doses of Bexsero given 2 months apart.
Eligibility for the meningococcal B immunisation programmeFollowing review of the
epidemiological and economic evidence as well as vaccine safety and efficacy, the JCVI
recommended that young infants were prioritised with the aim of providing optimal protection as
early as possible because they have the highest disease incidence.
The meningococcal B vaccine, Bexsero, became available through General Practitioner (GP)
services from the 1 September 2015. Infants attending their GP practice for their routine primary
immunisations at 8 weeks and 16 weeks of age should be offered meningococcal B vaccine
along with their routine infant immunisations followed by a booster on or after their first birthday.
Children remain eligible to receive Bexsero vaccine until they reach 2 years of age.
If the course is started late, the interval between doses can be reduced to 4 weeks to ensure 2
doses of vaccine can be administered before the infant reaches 2 years of age.
MenB vaccine is not indicated for children after their second birthday unless they are in a risk
group (as defined in the green book chapter 7 and chapter 22).
Catch-up programme
When the MenB vaccination programme commenced on 1 September 2015, a limited
opportunistic catch-up (without active recall) was implemented for those infants born between
01 May 2015 and 30 June 2015.
Infants born before 1 May 2015
After reviewing the cost-effectiveness model, the JCVI did not recommend a catch-up
programme for infants born before 1st May 2015. As the vaccine was only found to be cost-
effective at a very low price, a sustainable approach had to be followed for implementation. As
meningococcal disease peaks around 5 months of age, the priority of the MenB immunisation
programme is to ensure that Bexsero is offered routinely to infants before the peak in incidence
of disease.
Children born before 1 May 2015 are not eligible for the MenB vaccine unless they are in a
clinical risk group.
Meningococcal B vaccination. Information for healthcare professionals
10
Infants aged 6 to 8 weeks of age
Infants may receive their first dose of primary immunisations from 6 weeks of age in exceptional
circumstances (such as pre-travel) but it is not routinely recommended to offer infants their
primary immunisations before 8 weeks of age.
Bexsero vaccine is licensed from 8 weeks of age. If administered to infants between 6 and 8
weeks of age, a patient specific direction (PSD) will be required as the patient group direction
(PGD) does not include infants younger than 8 weeks of age. Parents should also be informed
that paracetamol prescribing guidance will usually advise that infants younger than 2 months of
age should not receive paracetamol. As paracetamol is recommended to be administered
around the time of Bexsero vaccination, the advice in Table 1 should be followed and infants
aged 6 to 8 weeks of age should receive the same dose of infant paracetamol suspension
(2.5mls) as an 8-week old baby.
Parents should be provided with the PHE leaflet on paracetamol use and reassured that
paracetamol is given to infants younger than 2 months of age when clinically required (for
example to infants in SCBU and those admitted to hospital in the first few weeks of life).
Children 2 years of age and older
If Bexsero vaccine is clinically indicated for those aged 2 years and older (for example for those
with asplenia, splenic dysfunction or complement disorders), the vaccine can be administered
but must be sought separately from the national immunisation stock and there will be no
reimbursement as part of the national programme.
Some parents may opt to make alternative arrangements to have their child immunised with the
MenB vaccine if their child does not meet the eligibility criteria for the routine programme.
Parents should be informed that if the vaccine is not clinically indicated and a private
arrangement is made for vaccination, the provider may charge for the service as this
arrangement is outside of the national programme.
Meningococcal B vaccination. Information for healthcare professionals
11
Adverse reactions commonly associated with the administration of Bexsero
In clinical trials, the most common adverse reaction observed in infants and children under 2
years of age was a high rate of fever (>38°C) when Bexsero was administered with the other
routine childhood vaccines (see pages 13 to 15).
Other very common adverse reactions (occurring in more than 1 in 10 children), observed in
infants and children (up to the age of 10 years) are tenderness at the injection site (including
severe tenderness defined as crying when moving injected limb), rash, swelling or induration at
the injection site, irritability, change in feeding or eating, sleepiness and unusual crying.
Bexsero is no longer subject to additional monitoring under the black triangle () labelling
scheme by the Medicines and Healthcare Regulatory Agency (MHRA) but all suspected
adverse reactions should continue to be reported to the MHRA using the Yellow Card scheme.
Latex allergy
The tip cap of the syringe may contain natural rubber latex. Although the risk for developing
allergic reactions is very small, healthcare professionals should consider the benefit-risk prior to
administering this vaccine to subjects with known history of hypersensitivity to latex. For latex
allergies other than anaphylactic allergies (for example a history of contact allergy to latex
gloves), vaccines supplied in vials or syringes that contain latex can be administered.
For a full list of excipients, healthcare professionals should read the manufacturers’ Summary of
Products Characteristics (SPC).
Prophylactic paracetamol
Following vaccination, infants may experience symptoms such as fever, irritability and reduced
appetite. Infants receiving prophylactic paracetamol when Bexsero is administered with routine
immunisations are less likely to experience these symptoms.
Fever and the use of prophylactic paracetamol after vaccination
Fever after vaccination with or without Bexsero is common and nearly always under 39oC.
Fever is a normal and expected response of the immune system against the vaccine antigens
and is generally not harmful but parents are often concerned about the risk of febrile
Meningococcal B vaccination. Information for healthcare professionals
12
convulsions or ‘fever fits’. Typically, febrile convulsions occur from 6 months to 5 years of age
and are very uncommon in younger age groups. In clinical trials involving several thousand
infants receiving their routine vaccinations (including Bexsero), febrile convulsions were very
rarely reported. In one of the largest Bexsero trials, Gossger and others (5) recruited and
vaccinated 1,885 infants at 4 different visits without paracetamol prophylaxis and only one infant
developed a febrile convulsion 2 days after receiving Bexsero. In the subsequent study of 364
infants receiving Bexsero with or without paracetamol, Prymula and others (6) reported that
there wasn’t a single case of febrile convulsion after any of the 4 vaccination visits.
If a parent suspects that their infant has had a convulsion or another serious reaction following
administration of any vaccine, including Bexsero, they should be advised to seek medical
attention and report it via the Yellow Card Scheme.
Risk of fever when Bexsero is administered at the same time as other routine childhood vaccines
In one clinical trial, fever (≥38°C) was reported in 51% to 62% of infants receiving Bexsero and
routine vaccines administered together although high fever (≥39°C) was less common (6 to
12%). Overall, fever (≥38.0°C) after any vaccination was reported in 76% of infants receiving
Bexsero and routine vaccines together, compared to 51% in infants receiving the routine
vaccinations alone. However, only 6 of the 1,885 recruited infants attended hospital because of
fever within 2 days after vaccination with Bexsero in this study.
In the study conducted by Prymula and others (6), 70% of infants receiving Bexsero had fever
(≥38.5°C) at least once in the first 3 days after any primary dose. Fever was less common
(39%) in infants receiving prophylactic paracetamol just before, or at the time of vaccination,
followed by 2 further administrations by parents or guardians at 4 to 6 hour intervals after
vaccination. Around 5% of infants receiving paracetamol had fever (≥39oC) and the frequency of
medically attended fever within 3 days of vaccination was ≤2% for any vaccination visit,
irrespective of whether Bexsero was administered alone or with the routine vaccinations. The
Prymula et al study was also important because it showed that responses to Bexsero and the
routine vaccinations were not affected by administering prophylactic paracetamol at the time of
vaccination.
In another vaccine study that assessed the effect of medications to prevent fever following the
pneumococcal conjugate vaccine Prevenar 13 (which did not include Bexsero) (7), infants
receiving 3 doses of paracetamol (at vaccination and at 6 to 8 hour intervals) were half as likely
to develop post-vaccination fever, and also half as likely to develop high fever (>39oC), when
compared with infants receiving 2 doses of paracetamol (first dose at 6 to 8 hours after
vaccination and another 6 to 8 hours later). This indicates that the greatest benefit in reducing
post-vaccination fever appears to come from the paracetamol dose given around the time of
vaccination.
Meningococcal B vaccination. Information for healthcare professionals
13
For the Bexsero programme, the JCVI has recommended 3 doses of paracetamol to be given to
infants receiving Bexsero with their routine primary immunisations at 8 weeks and 16 weeks.
Prophylactic paracetamol is not recommended for the 12-month boosters because the infants
are older and rates of fever are similar with and without Bexsero administration at this age.
Guidance on the use of liquid prophylactic paracetamol can be found below.
Some babies may still develop fever after vaccination, even after taking paracetamol. Parents
can be advised that if their baby still has a fever after the first 3 doses of paracetamol but is
otherwise well, they can continue to follow PHE post-immunisation paracetamol dosing
recommendations (also see page 18, Paracetamol product licencing). There should always be
at least 4 hours between doses and they should never give more than 4 doses in a day. The
child should also be kept cool by making sure they don’t have too many layers of clothes or
blankets on, and they should be offered plenty of fluids. If there are any concerns about the
baby at any time, advice should be taken from a GP or by calling 111. Information on the use of
ibuprofen for post vaccination fever can be found on page 19.
If Bexsero is administered separately to other routine primary immunisations (for example at a
different appointment), liquid paracetamol is not needed as the risk of fever is reduced.
Using prophylactic infant paracetamol suspension with Bexsero vaccine
As fever has been a very common adverse reaction in trials and in light of concerns raised that
an increase in fever may have a detrimental impact on the uptake of future immunisations, the
JCVI issued a position statement which recommended the use of prophylactic paracetamol at
the time of immunisation with Bexsero.
The JCVI also advised that parents and healthcare professionals need to be informed and
updated about the change in advice regarding the use of prophylactic paracetamol and the
reactogenicity of Bexsero when administered concomitantly with other routine childhood
immunisations to reduce any anxiety or concern.
This is a change to previous advice whereby the prophylactic use of antipyretics was not
routinely recommended as there was some evidence that they lowered the immune response to
some of the routine infant vaccinations. Additionally, it was also felt that a low grade fever was
to be expected following immunisation and such a response was an indication that the vaccine
was triggering the appropriate immunological response. The latter remains true. However, the
incidence of fever greater than 38°C when Bexsero is administered at the same time as other
childhood vaccines is greatly increased.
Meningococcal B vaccination. Information for healthcare professionals
14
Additionally, studies have shown that giving a dose of paracetamol around the time of
vaccination followed by a further 2 doses at 6 to 8 hourly intervals significantly reduced the rates
of fever associated with vaccination without affecting the immunogenicity of Bexsero or other
routine infant vaccines.
It is recommended that parents should be advised to give 2.5ml (120mg/5ml) of infant
paracetamol to their babies around the time of immunisation or as soon as possible after the
vaccines are administered, and to give 2 further doses at 4 to 6 hourly intervals (Table 1).
Infants aged 6 to 8 weeks of age who are receiving a first dose of Bexsero early (for example
infants travelling to another country before they reach 8 weeks of age), should receive infant
paracetamol suspension as described in Table 1 for infants aged 8 weeks.
Prophylactic paracetamol is not recommended for the 12 month boosters because the infants
are older and rates of fever are similar with and without Bexsero administration at this age.
Table 1. Dosage and timing of infant paracetamol suspension (120mg/5ml) for the
routine immunisation programme at 8 and 16 weeks*
Age of baby Dose 1 Dose2 Dose 3
8 weeks One 2.5ml
At the time of or as soon
as possible after
vaccination
One 2.5ml
4 to 6 hours after 1st
dose
One 2.5ml
4 to 6 hours after 2nd
dose
16 weeks One 2.5ml
At the time of or as soon
as possible after
vaccination
One 2.5ml
4 to 6 hours after 1st
dose
One 2.5ml
4 to 6 hours after 2nd
dose
*For premature babies, the dose should be calculated according to the infant’s weight
around the time of vaccination.
Recommendations for premature babies
Infants born at <32 weeks gestation should receive the vaccine at the appropriate chronological
age (age from date of birth) without correction for prematurity. The dose of prophylactic
paracetamol should be calculated according to the infant’s weight around the time of
vaccination.
Meningococcal B vaccination. Information for healthcare professionals
15
Alerting parents to the need to buy paracetamol prior to vaccination
Healthcare professionals should provide parents with the PHE meningococcal B vaccine leaflet
before their infant’s 8 week primary vaccination appointment (for example when the parents
register their baby at the practice or when they attend the 6 to 8 week check). This will alert
parents to the need to buy liquid paracetamol in preparation for the 8 week immunisation
appointment.
When the programme was introduced, practices were able to order liquid paracetamol sachets
and accompanying syringes via ImmForm. These are no longer available and parents should be
instructed to purchase infant strength liquid paracetamol and ensure that they are able to
administer the recommended doses of paracetamol at the time of vaccination and at home for
the next 2 days if needed (following both the first and third sets of primary immunisations at 8
and 16 weeks of age). Most local pharmacies, supermarkets and many local stores stock infant
liquid paracetamol suspension.
Paracetamol product licencing
The Commission on Human Medicines (CHM) was consulted regarding the previous licencing
restriction on Pharmacy (P) and General Sales List (GSL) paracetamol products which advised
consulting a GP or pharmacist if more than 2 doses were required for an 8 week old infant post-
immunisation. This was to ensure early diagnosis of systemic bacterial infection.
The licence was updated during 2016 and supports the PHE recommendations for paracetamol
use following MenB vaccination (also see Table 1 above).
This recommendation is based on the likelihood that fever is due to immunisation. This
recommendation does not extend to fever at any other time and if the infant is otherwise unwell
parents should trust their instincts and not delay seeking medical attention for their infant.
Parents can be reassured that it is appropriate to follow PHE post-immunisation paracetamol
dosing recommendations. Advice on bottles and sachets of infant paracetamol has now been
changed to reflect the recommendation that paracetamol can be given for relief of fever after
vaccinations from 2 months of age. In the event that Bexsero is required to be administered to
an infant aged 6 to 8 weeks, the paracetamol recommendations in Table 1 should be followed.
Meningococcal B vaccination. Information for healthcare professionals
16
Liquid paracetamol supply
Nurses and midwives can only supply or administer medicines using a recognised process.
Standards for medicines management that were previously issued by the Nursing and Midwifery
Council (NMC) were withdrawn in January 2019 but guidance on where to find further
information on the safe and effective handling, management and administration of medicines is
available on the NMC website.
When the Men B vaccination programme was introduced, Public Health England (PHE) made
available a Homely Remedy Protocol for the supply of liquid infant paracetamol. This expired on
31 August 2017 and there is no longer a central supply of liquid paracetamol for infants having
MenB vaccination. Nurses should advise parents that they need to ensure that they have liquid
paracetamol available for their infant at the time of vaccination and at home for the next 2 days
if needed.
Ibuprofen as an alternative to paracetamol to reduce post-vaccination fever after Bexsero
In a head-to-head clinical trial of prophylactic paracetamol versus ibuprofen to reduce post-
vaccination fever, ibuprofen (2 or 3 doses) did not reduce the rate or intensity of post-
vaccination fever compared to the control arm where infants did not receive any anti-pyretic.
This suggests that paracetamol should be the only recommended prophylactic anti-pyretic to
reduce post-vaccination fever in infants. For this reason, ibuprofen should not be used as an
alternative to prophylactic paracetamol at the time of vaccination, but can be used for treatment
if the infant subsequently develops a post-vaccination reaction, including fever. If an infant still
has a fever 48 hours after vaccination or if parents are concerned about their infant’s health at
any time, then advice should be taken from a GP or NHS 111.
Incomplete dose of liquid paracetamol
If the infant spits out or regurgitates at least half of the paracetamol suspension, then an
additional dose (one dose of 2.5ml spoonful) of liquid paracetamol should be administered. If
the second dose is spat out, do not give a third dose.
Meningococcal B vaccination. Information for healthcare professionals
17
Administering oral rotavirus vaccine at the same time as liquid paracetamol
If possible, give Rotarix vaccine and prophylactic paracetamol with a short interval between
them. Although the live vaccine virus is unlikely to be affected by close sequential administration
of a small volume of paracetamol syrup, leaving a short interval between the vaccine and the
paracetamol syrup may reduce the chance of the rotavirus vaccine being vomited back up.
Vaccine preparation and administration
Preparing Bexsero vaccine
The vaccine comes in a box that contains a prefilled syringe with a volume of 0.5mls. During
storage, the contents of the syringe may settle with off-white deposits being noticeable. Before
use, the pre-filled syringe must be shaken well so that any observable deposits are thoroughly
mixed into the liquid, forming a homogenous suspension that should be administered
immediately. The vaccine should not be administered where there are variations in physical
appearance (such as having the appearance of a non-homogenous suspension) or there are
signs of foreign particulate observed after shaking.
When newly licensed, Bexsero vaccine was subject to additional monitoring under the black
triangle labelling scheme by the Medicines and Healthcare Regulatory Agency (MHRA).
Although this vaccine no longer has black triangle status, it is recommended that it continues be
administered on its own into the anterolateral aspect of the left thigh via intramuscular injection.
This is to enable accurate monitoring of local reactions which can then be reported to the MHRA
using the Yellow Card Scheme.
Administering Bexsero vaccine with other vaccines
Bexsero can be given at the same time as, or at any interval from, all of the other vaccines
administered as part of the routine childhood immunisation programme.
Meningococcal B vaccination. Information for healthcare professionals
18
Bexsero vaccine contraindications
There are very few infants who cannot receive meningococcal vaccines. Where there is doubt,
instead of withholding immunisation, appropriate advice should be sought from a consultant
paediatrician with immunisation expertise, a member of the Screening and Immunisation team
or from the local PHE health protection team.
Bexsero should not be administered to those who have had:
• a confirmed anaphylaxis to a previous dose of the vaccine OR
• a confirmed anaphylaxis to any constituent or excipient of the vaccine
For the composition and full list of excipients of the vaccine, please refer to the manufacturer’s
Summary of Product Characteristics (SPC).
Administering Bexsero to infants less than 12 months of age
When Bexsero was introduced to the national vaccination programme, it was recommended
that the vaccine be administered via intramuscular (IM) injection into the anterolateral aspect of
the left thigh, ideally on its own, so that any local reactions could be monitored more accurately.
If another vaccine needs to be administered in the same limb, then they must be given at least
2.5cm apart. The site at which each vaccine is given should be noted in the individual’s health
records.
Administering Bexsero at 12 months of age
Infants attending for their routine booster immunisations at 12 months are likely to receive at
least 4 vaccines at that same appointment. It is recommended that Bexsero should be
administered in the left thigh, ideally on its own, with other booster immunisations being
administered into the remaining 3 limbs. If another vaccine needs to be administered in the
same limb, then it must be given at least 2.5cm apart. The sites at which each vaccine was
given should be noted in the individual’s health records.
Healthcare professionals are encouraged to discuss any recent immunisations at the 12 month
booster appointment with parents. This is because some infants may receive additional
vaccines, such as Hepatitis B and BCG, as part of a selective immunisation programme at
around 12 months of age and additional vaccines should not be administered into the same limb
as the BCG vaccine for a period of 3 months from administration.
Meningococcal B vaccination. Information for healthcare professionals
19
Administering multiple vaccines in one session
Some parents may be concerned about the number of vaccines being administered in one
session, particularly at 12 months of age when 4 vaccines are scheduled to be administered.
Whilst these concerns are understandable, parents should be reassured by confident and
knowledgeable healthcare professionals that the aim of immunisation is to provide protection
against harmful diseases at the very earliest opportunity. The Centres for Disease Control and
Prevention (CDC) advise that there are no harmful effects from administering multiple vaccines
in one session and there is no evidence to support arguments of overloading the immune
system. From the moment a child is born, they are continually being exposed to a huge number
of bacteria and viruses on a daily basis that the immune system is able to cope with.
Additionally, administering multiple vaccines in one session is a routine occurrence in most
countries around the world with no evidence of harmful effects.
Parents who request for their child’s immunisations to be separated should be informed of the
potential risks of delaying protection against a disease. Additionally healthcare professionals are
encouraged to identify the reasons for such requests as many parents may be concerned about
the number of vaccines administered in one session. Such parents can be reassured that
studies have clearly demonstrated that there are no harmful effects of administering more than
one vaccine in one session. Parents can also be reassured that offering multiple vaccines in this
way is a routine occurrence around the world with no harmful effects being identified.
Delaying vaccination
Parents should be discouraged from delaying immunisation as this inevitably delays important
protection. The immunisation schedule has been designed to ensure optimal protection against
diseases that are most common in the very young such as pneumococcal disease, Hib,
meningococcal disease and pertussis (whooping cough). These diseases can be life-
threatening and it is important for children to receive protection at the earliest possible
opportunity.
Administering Bexsero at the same time as MenC or MenACWY vaccines
Findlow and others (8) conducted a phase II trial in healthy adult laboratory workers which
explored the safety and immunogenicity of 4CMenB and MenACWY-CRM when administered
concomitantly. This trial concluded that concomitant use is both safe and immunogenic.
A clinical trial conducted by Sadafi and others (9) during which children received the
meningococcal B vaccine co-administered with MenC conjugate vaccine in South America,
found that immune responses to both the MenB and MenC vaccines were satisfactory and
Meningococcal B vaccination. Information for healthcare professionals
20
although reactogenicity was higher for concomitant vaccine administration, did not identify any
safety concerns. Since Bexsero is a protein-based vaccine and both MenC and MenACWY are
polysaccharide conjugate vaccines with no shared antigens, interference with vaccine
responses is unlikely.
Therefore, currently available evidence indicates that Bexsero can be safely co-administered
with MenC and MenACWY conjugate vaccines and other conjugate vaccines (for example
pneumococcal and Hib vaccines) without affecting the immune response to either vaccine.
Vaccine administration errors
Bexsero administered earlier than 8 weeks of age
The immunisation schedule has been designed to provide early protection against infections
that are most dangerous for the very young. Recommendations for the age at which vaccines
should be administered are informed by the age-specific risk for a disease, the risk of
complications and the ability to respond to the vaccine. Therefore, vaccines should be
administered as closely to the schedule as possible.
In certain circumstances, the first set of primary immunisations (including MenB) can be
administered from 6 weeks of age, for example for infants that are due to travel to another
country before they reach 8 weeks of age when the primary immunisations are usually given.
However, Bexsero is licensed for use from the age of 8 weeks so if it is administered earlier
than this, it should be treated as an ‘off-label’ uses of a licensed vaccine and will require a
patient specific direction (PSD) for its supply and administration.
If Bexsero is inadvertently given prior to 8 weeks of age but the infant is over 6 weeks of age,
this should count as a valid dose and does not need to be repeated. Doses given before 6
weeks of age should be discounted and the scheduled infant doses should still be given at 8
and 16 weeks of age.
Inadvertent early administration of second dose
In the event that the second dose of Bexsero is inadvertently administered earlier than
recommended (for example with the 12 week immunisations), infants should be offered an
additional dose of vaccine at 16 weeks to ensure protection against meningococcal B disease.
Meningococcal B vaccination. Information for healthcare professionals
21
As Bexsero has been associated with an increase in fever when administered concomitantly
with other routine childhood vaccines, infants inadvertently given Bexsero at 12 weeks should
be given liquid paracetamol as recommended for the 8 week or 16 week Bexsero dose.
For further information, please refer to the sections titled Adverse reactions commonly
associated with the administration of Bexsero and Using prophylactic infant paracetamol
suspension with Bexsero vaccine.
Missed doses of Bexsero vaccine
MenB vaccination is offered to children up to their second birthday. Infants who have missed
scheduled doses of MenB, or who have not received the recommended number of doses for
their age, should be offered the vaccine at the earliest opportunity. These infants should be
managed according to the vaccination of individuals with uncertain or incomplete immunisation
status” algorithm to ensure they are up to date with all immunisations.
1. Infants younger than 12 months should receive 2 doses of MenB vaccine, ideally 2 months
apart. If the infant does not commence their MenB immunisation course before the age of
10 months, this interval can be reduced to 4 weeks to enable 2 doses of vaccine to be given
before their first birthday. These infants should then follow the routine schedule and receive
a booster dose in their second year of life. The booster dose is recommended to be given
around the time of the first birthday but if primary doses have been given late, a minimum 4
week interval between primary and booster doses should be observed.
2. Children aged one year to less than 2 years who have never had Men B vaccine should
receive 2 doses of vaccine with an 8 week interval between doses.
3. Children aged one year to less than 2 years who only received 1 dose of MenB vaccine in
their first year of life should receive 2 doses of vaccine in their second year of life. Ideally an
8 week interval should be observed between doses but this interval can be reduced to a
minimum of 4 weeks to ensure the doses can be administered before the child’s second
birthday, for example, if the first of these 2 doses is not given until the child is 22 months
old.
Meningococcal B vaccination. Information for healthcare professionals
22
Vaccine inadvertently administered to child born before 1 May 2015
Children born before 1 May 2015 are not recommended to receive Bexsero and should not be
offered additional meningococcal B vaccinations unless they are in one of the identified risk
groups recommended to receive the vaccine (asplenia, splenic dysfunction or complement
disorders). Healthcare professionals should reassure parents that no further action is required
and should report the administration error via their local governance system(s) so that
appropriate action can be taken, lessons can be learnt and the risk of future errors minimised.
Incomplete dose administered
In the event that less than the recommended dose of Bexsero is administered, the vaccination
will need to be repeated because the dose that the infant received may not be sufficient to
evoke a full immune response. Where possible, the dose of Bexsero should be repeated on the
same day as the incomplete dose was administered.
In the event that the additional dose of Bexsero cannot be administered at the same visit or on
the same day, arrangements should be made to administer the replacement dose as soon as
possible, in order not to delay protection.
As Bexsero has been associated with an increase in rates of fever when administered
concomitantly with other childhood vaccines, prophylactic paracetamol should be offered with
replacement Bexsero doses if offered at the same time as other vaccines. For further
information, please refer to the sections titled ‘Adverse reactions commonly associated with the
administration of Bexsero’ and ‘Using prophylactic infant paracetamol suspension with Bexsero
vaccine’.
Meningococcal B vaccination. Information for healthcare professionals
23
Useful links
Public Health England and NHS England. Introduction of meningococcal B immunisation for
infants
www.gov.uk/government/publications/menb-vaccination-introduction-from-1-september-
2015
Public Health England. Immunisation against infectious diseases: meningococcal chapter 22.
www.gov.uk/government/publications/meningococcal-the-green-book-chapter-22
Bexsero vaccine PGD
www.gov.uk/government/publications/menb-vaccine-bexsero-patient-group-direction-
pgd-template
Clinical and public health management of meningococcal disease
www.gov.uk/guidance/meningococcal-disease-clinical-and-public-health-management
Meningococcal B (MenB) vaccination programme documents and resources
www.gov.uk/government/collections/meningococcal-b-menb-vaccination-programme
Men B vaccine coverage estimates
www.gov.uk/government/publications/meningococcal-b-immunisation-programme-
vaccine-coverage-estimates
Meningitis Research Foundation
www.meningitis.org/
Meningitis Now
www.meningitisnow.org/
NHS UK Meningitis overview
www.nhs.uk/conditions/Meningitis/Pages/Introduction.aspx
Joint Committee on Vaccination and Immunisation www.gov.uk/government/groups/joint-
committee-on-vaccination-and-immunisation
British Society for immunology
www.immunology.org/public-information
Meningococcal B vaccination. Information for healthcare professionals
24
References 1. Public Health England Health Protection Report. ‘Invasive meningococcal disease
(laboratory reports in England)’ Volume 9 number 38 (Viewed on 13 May 2021)
2. Bexsero Summary of Product characteristics (SPC) available at www.medicines.org.uk/emc/product/5168/smpc (Viewed 20 2021)
3. Parikh S, Andrews N, Beebeejaun K and others. ‘Effectiveness and impact of a reduced infant schedule of 4CMenB vaccine against group B meningococcal disease in England:a national observational cohort study’ Lancet December 2016 3;388(10061): pages 2775-2782.Abstract available at: www.ncbi.nlm.nih.gov/pubmed/28100432 (Viewed on 13 May 2021)
4. Ladhani S and others ‘Vaccination of Infants with Meningococcal Group B Vaccine
(4CMenB) in England’ The New England Journal of Medicine: volume 382, pages 309-317 (Viewed on 13 May 2021)
5. Gossger N and others European MenB Vaccine Study Group. ‘Immunogenicity and Tolerability of Recombinant Serogroup B Meningococcal Vaccine Administered With or Without Routine Infant Vaccinations According to Different Immunization Schedules: A Randomized Controlled Trial’ JAMA. 2012 February 8307(6), pages 573-582 (Viewed on 13 May 2021)
6. Prymula R and others. ‘A phase 2 randomised controlled trial of a multicomponent
meningococcal serogroup B vaccine (I)’ Human Vaccine and Immunotherapy 2014 10(7), pages 1993-2004 (Viewed 13 May 2021)
7. ClinicalTrials.gov (2014). ‘Study assessing the effect of medications to prevent fever on Prevenar 13’ (outcomes 18-21) (Viewed on 13 May 2021)
8. Findlow J and others. ‘Safety and immunogenicity of a four-component meningococcal
group B vaccine (4CMenB) and a quadrivalent meningococcal group ACWY conjugate vaccine administered concomitantly in healthy laboratory workers’ Vaccine (2015): Volume 13 issue 29, pages 3322-3330 (Viewed 13 May 2021)
9. Safadi M and others. ‘Immunogenicity and safety of concomitant administration of meningococcal serogroup B (4CMenB) and serogroup C (MenC-CRM) vaccine in infants: a phase 3 randomised controlled trial’ Vaccine 11 April 2017, Volume 35 issue 16, pages 2052-2059 (Viewed 13 May 2021)
25
Published July 2021
PHE gateway number: GW-8835
www.gov.uk/phe
Twitter: @PHE_uk
www.facebook.com/PublicHealthEngland
© Crown copyright 2021
For queries relating to this document, please contact: [email protected]